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dc.contributor.author정낙신-
dc.contributor.author이상국-
dc.contributor.author최원준-
dc.date.accessioned2016-11-25T02:11:29Z-
dc.date.available2016-11-25T02:11:29Z-
dc.date.issued2008-
dc.identifier.issn1746-8272-
dc.identifier.otherOAK-18113-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/232816-
dc.description.abstract4-Seleno analogue of 1-beta-arabinofuranosyl cytosine (ara-C) was synthesized via 4'-selenouridine as a key intermediate, which was easily prepared from D-ribose. The arabino configuration was achieved by chemoselective ring opening of the 2,2'-anhydro-4'-selenouridine. The synthesized 4'-seleno-ara-C showed potent antitumor activity (IC(50) = 1.5 microM) against stomach cancer cells (SNU638).-
dc.languageEnglish-
dc.titleSynthesis and antitumor activity of 1-beta-4-selenoarabinofuranosyl cytosine (4'-seleno-ara-C).-
dc.typeArticle-
dc.relation.issue52-
dc.relation.indexSCOPUS-
dc.relation.startpage639-
dc.relation.lastpage640-
dc.relation.journaltitleNucleic acids symposium series (2004)-
dc.identifier.scopusid2-s2.0-78649436192-
dc.author.googleLee H.-
dc.author.googleTosh D.K.-
dc.author.googleChoi W.J.-
dc.author.googleKim Y.M.-
dc.author.googleLee S.K.-
dc.author.googleJeong L.S.-
dc.contributor.scopusid정낙신(16028528200)-
dc.contributor.scopusid이상국(36067620500)-
dc.contributor.scopusid최원준(55732412300;57211762651)-
dc.date.modifydate20230627112239-
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약학대학 > 약학과 > Journal papers
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